FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

STERIGAUZE GEL DRESSING

K Number: K952419 · Decision Jul 26, 1995
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
144
Applicant Total
12
Review Days
64

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Basic Information

Device Name
STERIGAUZE GEL DRESSING
K Number
K952419
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Acacia Laboratories, Inc.
Date Received
May 23, 1995
Decision Date
July 26, 1995
Product Code
MGQ
Advisory Committee
Unknown
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MGQ Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MGQ), ordered by most recent decision date.

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Other Clearances by Acacia Laboratories, Inc.

K Number Device Name
K952420 STERIGAUZE WET DRESSING
K951861 STERICARE WOUND CARE GEL
K952414 PREFILLED SYRINGE FOR INFLATION OF FOLEY CATHETER
K951914 HYDRACARE ABSORBENT WOUND DRESSING
K950344 HORIZON FOLEY CATHETERIZATION TRAY WITHOUT CATHETER
K913408 STERILE PLASTIC DRAPE
K901761 STERILE SUCTION TUBING SET
K892856 NEWMARK(TM) CORONARY ARTERY BYPASS GRAFT MARKERS
K892804 NEWCHILL(TM) CARDIAC INSULATOR
K884055 SURGI-TAG(TM) STERILE LABEL SETS
Search all 12 clearances from Acacia Laboratories, Inc. →